Product Recalls in Kentucky

Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 934 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
934 in last 12 months

Showing 43081–43100 of 51,386 recalls

DrugJuly 9, 2014· Gyma Laboratories Of Amer,Inc

Recalled Item: Propranolol HCl Recalled by Gyma Laboratories Of Amer,Inc Due to cGMP...

The Issue: cGMP Deviations: GYMA laboratories Inc. has recalled multiple Active...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2014· Gyma Laboratories Of Amer,Inc

Recalled Item: Clonidine HCL Recalled by Gyma Laboratories Of Amer,Inc Due to cGMP...

The Issue: cGMP Deviations: GYMA laboratories Inc. has recalled multiple Active...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2014· Gyma Laboratories Of Amer,Inc

Recalled Item: Dipyridamole API Recalled by Gyma Laboratories Of Amer,Inc Due to cGMP...

The Issue: cGMP Deviations: GYMA laboratories Inc. has recalled multiple Active...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 9, 2014· Richard Wolf Medical Instruments Corp.

Recalled Item: The Hulka Clip is a sterile packaged medical device that Recalled by Richard...

The Issue: Richard Wolf Medical Instrument Corporation is recalling Hulka Clip Tubal...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Philips Ultrasound, Inc.

Recalled Item: QLAB 10.1 Core Module PN 453561728001. QLAB Quantification Software is...

The Issue: The QLAB a2DQ and aCMQ features have a defect that may use incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Teleflex Medical

Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...

The Issue: The temperature probe does not properly connect to the temperature port.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Nanosphere, Inc.

Recalled Item: Verigene BC-GN Test Kit (Catalog number 20-005-021) includes: 1) 20 Recalled...

The Issue: Nanosphere Inc. has recently determined through four customer complaints...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Philips Ultrasound, Inc.

Recalled Item: QLAB 10 Core Module PN 453561704771. QLAB Quantification Software is...

The Issue: The QLAB a2DQ and aCMQ features have a defect that may use incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Teleflex Medical

Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...

The Issue: The temperature probe does not properly connect to the temperature port.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Teleflex Medical

Recalled Item: Emerald Fiberoptic Blade Recalled by Teleflex Medical Due to Packaging...

The Issue: Packaging Error: Customers have reported receiving incorrect product. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Carestream Health, Inc.

Recalled Item: Kodak DirectView DR 7500 Diagnostic X-Ray System Product Usage: The Recalled...

The Issue: An on-site evaluation of the equipment parts that attach the Beta Assembly...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2014· Gyrus Medical, Inc

Recalled Item: Gyrus ACMI Falope-Ring Dilator Recalled by Gyrus Medical, Inc Due to...

The Issue: Falope-Ring Dilator for Reusable Falope-Ring Band Applicators have been sold...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 8, 2014· Pfizer Inc.

Recalled Item: VIRACEPT (R) (nelfinavir mesylate) Tablets Recalled by Pfizer Inc. Due to...

The Issue: Labeling: Incorrect or missing lot and or Exp Date: The bottles were labeled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodJuly 8, 2014· Michael Foods, Inc.

Recalled Item: Shell Eggs packaged under the following labels: (1) Abbotsford Farms...

The Issue: Shell eggs contaminated with Pseudomonas fluorescens.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodJuly 8, 2014· Seoul Shik Poom, Inc.

Recalled Item: Choripdong Chocolate Almond Richmond Ice Bar 4 bars/432 mL Seoul Recalled by...

The Issue: Seoul Trading USA Inc. is recalling Choripdong Chocolate Almond Richmond Ice...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Immunodiagnostic System --- For use in the in vitro quantitative...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: 4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4001S Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing